What is "thiol"

n. (context organic chemistry English) a univalent organic radical (-SH) containing a sulphur and a hydrogen atom; a compound containing such a radical

In organic chemistry, a thiol (, ) is an organosulfur compound that contains a carbon-bonded sulfhydryl or sulphydryl (–C–SH or R–SH) group (where R represents an alkyl or other organic substituent). Thiols are the sulfur analogue of alcohols (that is, sulfur takes the place of oxygen in the hydroxyl group of an alcohol), and the word is a portmanteau of "thion" + "alcohol," with the first word deriving from Greek θεῖον (theion) = "sulfur". The –SH functional group itself is referred to as either a thiol group or a sulfhydryl group.

Many thiols have strong odors resembling that of garlic or rotten eggs. Thiols are used as odorants to assist in the detection of natural gas (which in pure form is odorless), and the "smell of natural gas" is due to the smell of the thiol used as the odorant.

Thiols are sometimes referred to as mercaptans. The term mercaptan was introduced in 1832 by William Christopher Zeise and is derived from the Latin mercurium captāns (capturing mercury) because the thiolate group bonds very strongly with mercury compounds."Mercaptan" (ethyl thiol) was discovered in 1834 by the Danish professor of chemistry William Christopher Zeise (1789–1847). He called it "mercaptan", a contraction of "corpus mercurium captans" (mercury-capturing substance) [p. 88], because it reacted violently with mercury(II) oxide ("deutoxide de mercure") [p. 92]. See:

• The article in Annales de Chimie et de Physique (1834) was translated from the German article:
• The article in Annalen der Physik und Chemie (1834) was translated from the original Danish article in:
• German translation is reprinted in:
• Summarized in: Thiols react with mercury to form mercaptides.